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作 者:左榘[1,2] 牛爱珍[1,2] 安英丽[1,2] 何炳林[1,2] 冉少峰[1,2] 梁德海[1,2]
机构地区:[1]南开大学吸附分离功能高分子材料国家重点实验室 [2]南开大学化学系
出 处:《高分子学报》1998年第4期419-423,共5页Acta Polymerica Sinica
基 金:国家自然科学基金
摘 要:在苯乙烯(St)二乙烯苯(DVB)自由基共聚的凝胶化反应过程中定时取样,得到凝胶化点前后及至终点的一系列样品,然后用激光光散射技术,包括研究散射光强及其角度依赖性的静态光散射(SLS)和研究散射光频移的动态光散射(DLS),表征了这系列样品的重均分子量Mw、均方旋转半径Rg、第二维利系数A2及流体力学半径Rh等静、动态参量及这些参量的变化规律。During the copolymerization of styrene with divinylbenzene,a series of samples were taken at different gelation time from the beginning to the end of this reaction.For sol samples before and after gelation point time Tg(=18 15h),the weight average molecular weight (M w), the mean square radius of gyration (R g) of the polymer chain in solution,the second virial coefficient (A 2),hydrodynamic radius (R h),parameter δ(=R g/R h) and the size distribution for these samples were determined by static light scattering and dynamic light scattering.Before T g,both M w and R g increase rapidly,then become divergence near T g and reach the maximum at Tg. R h almost follows the same way except not so rapidly.After T g,all go down.A 2 decrease gradually following the gelation.δ are 278,380 and 187 at 15h,18 25h and 29h,respectively,which agree with the rules of linear and branching polystyrene.The size distribution of these sol samples always were rather wide and before T g and after Tg,their diameters tend to increase and decrease,respectively.Based on these data,the evolution rules of these parameters were withdrawn and the quantitative characterization of span process of gelation was carried out successfully.
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